ZMP
LOC570502
Ensembl ID:
Human Orthologue:
KIF21B
Human Description:
kinesin family member 21B [Source:HGNC Symbol;Acc:29442]
Mouse Orthologue:
Kif21b
Mouse Description:
kinesin family member 21B Gene [Source:MGI Symbol;Acc:MGI:109234]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15402 | Nonsense | Available for shipment | Available now |
sa16362 | Essential Splice Site | Available for shipment | Available now |
sa13339 | Nonsense | Available for shipment | Available now |
sa21831 | Nonsense | Available for shipment | Available now |
sa6188 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41759 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21832 | Essential Splice Site | Available for shipment | Available now |
sa10974 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15402
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093108 | Nonsense | 60 | 1237 | 2 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 2881723)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2833361 |
GRCz11 | 11 | 2902715 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAAAGATAAAGCCTTCACGTATGACTTTGTRTTTGACCTGGATGCTCAT[C/T]AGCAGCAGATCTACAGCGCCTGCGTTCACAAGCTCATCGAGGGCTGCTTT
Long Flanking Sequence:
AAATTGAACATAGAAGGAAATCGTATCATACAAAACAACCTCAAGAATGTTTACATGCGATGACAGAGAGACTATTCATGTGCATGTCAGTTTACTGTATGAAGAATGAAATGGCCTTAAACAATAACTAAATGCACTACAGAATGTTACGTTTCACACAAATTGCACGTAAAACATCAATCTTTCGCAGTGTAATACTCGAGTGCTATTAAAAGGGCTACTTTTTACTCATACTTTGACTGTGGCAGATTTAGATTCTCAGAGATGTCAGTTCCCACATGACTAGGATGCCCCATATGGCCTTTATTTAACTAATAAGTTGTTTATATATTATTTATCTGATTTATTGCTGTTATCTTTCCAGGATCCGTCCTCAGATGGCGAAGGAGAAGATCGAGGGATGCCACATCTGCACCTCCGTCACTCCCGGCGAGCCGCAGGTGCTCTTGGGTAAAGATAAAGCCTTCACGTATGACTTTGTGTTTGACCTGGATGCTCAT[C/T]AGCAGCAGATCTACAGCGCCTGCGTTCACAAGCTCATCGAGGGCTGCTTTGAGGGATACAACGCTACCGTCTTCGCTTACGGACAGGTAACGGCTAGCAAACCCAGAAATGCAATTTAATAATGTGAGTACAGGGCCTAAAAAACTTTGTTTTCCTTGTCTTGTTCACATTGCAGACAGGCTCAGGAAAGACGTACACCATGGGCACTGGTTTTGACGTGAGCGTGTCGGAGGACGAGCAGGGGATCATCCCGCGGGCCGTACACCAGCTCTTTCAGGGCATCCAGAAACGCAGACTAGAGGCTCAGAGCGCAGACATCCCTCCGCCAGATTTCAAAGTCAGCGCACAGTTCCTGGAGGTGAGGCTACAACATGACTATCATACCATGCTGCCTATTTTTGAAGTAATGCTGTAGTTTTACTGTGAAATTGAACATTTGAGATGTGGGTGGGTGATATCGTTTCAATGTGTAAAAGTTCTACTGACGAAACAACGATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16362
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093108 | Essential Splice Site | 199 | 1237 | 4 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 2884907)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2836545 |
GRCz11 | 11 | 2905899 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCTACACCACTGGAGTGACCTCACGACTGGYCAGCTCAGAGGACGAGG[T/C]CAGATTGCCTTGTTTTGTTGTCTGAGCAYKAAAAGAATTCAAATTGACCA
Long Flanking Sequence:
GAAACCGGAGCACCTGGAGGAAATACACGCGAAGGCAGGGAGAACATGCAAACTCCACACAAATCTTTCCATTGAAGCATTTTTTTAATGGAATATCTCAAAATCCACAAAAAAATATGTGGACTGAAACATGGCTAATGATGACAGAATTTTCAGTTTTGGGTGAACTATCTCTTGTCTGTTTTTGTCATGAGCTTTATAAAGTTATTATTATTTCTCATGACTCAGCTTGTGTGGTCTGTGGGAATCAGAGGTCAAATATGCTGATTTCTGGCCCTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTCCTGCAGCTCTACAATGAGGAGATCCTGGACCTGTTTGACAGCACGCGTGATCCTGAGGCTCGAGGCCGGAAGTCCAATATTAAGATCCACGAAGACGGCAGCGGAGGAATCTACACCACTGGAGTGACCTCACGACTGGTCAGCTCAGAGGACGAGG[T/C]CAGATTGCCTTGTTTTGTTGTCTGAGCACTAAAAGAATTCAAATTGACCATATTTCATTCATTCATTCATTTTCTTCCGCTTATGCGGGGACTGGCCGCGGGGGCAAAAGTCTCAGGAGGGAACGCTACACTTCCTTCTACTCGTATCTCAAGGTGTTCCCAGGCTAGTCGAGAGACACATGATCCCTCCAGCATGTATTAAGGAGGCCTCCTCCTGGGGGCGCAAGCTTGAAATACCTCCCTTGGTAGGCGTCCAATTGGCATCTGAAACAGATGCCACAGCCACCTCAGCTGACTTCTCTCAATGTGGAGGAGCAGCGGCTCCACTCCGAGCTCCTCAGCTCCTCCCGGGTGACAGAGCTCCTCACCCTATCTATAAGGGTGCGCCCTGCCACCCTGCGAAGAAATTCATTTTTATTTCAGTTTGTATCCGAGATCTTGTCCTTTCGGTTATGAGCTGCATGTGTGGAGTTTGCATGTTCTCCCTGCGTTAGCGAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13339
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093108 | Nonsense | 383 | 1237 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 2893401)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2845039 |
GRCz11 | 11 | 2914393 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGCCCGCAACATCAAGAACAAGGTGATCGTCAACCAGGATAAAACCAGC[C/T]AGCAGATCAGCGCGTTACGAGCCGAGATCGCACGACTACAGATGGAGATC
Long Flanking Sequence:
CCCATATGCATTCATTTATCCTCCATGCAAAACTCCATGCAAAAAAACTTTTCTTCTGGAGTCAGCCGGTCTGCTTGGTCCCTCTCTAGTGCACACTGCAGTTGTTGTGCGCTGAAGGTTAATGCATGTACACAGTGTATATCAGAGGGTCACTCAGCCCACACGGGACGACACAGACAACCCATATATCCTCCTGATGTGGGTTCAGAGGGGGAGTTGATTGAATTAAACATGAGCGGCTGCAGACAGTGGCGCTGCTTTAAACGGATTCCGTCGCGTAACCATGAAACTATGCGGGCACCATGTGTGTGGTTGTGTTTATCTGTTTTGATCTCTTCTGAATGTCTTCTCGCTTTGTGTGTTTATCTAGTCGGACTGTGATGATTGCCTGCGTGAGCCCGTCTGATCGCGACTTCATGGAGACCCTGAACACGCTGAAGTATGCCAACCGGGCCCGCAACATCAAGAACAAGGTGATCGTCAACCAGGATAAAACCAGC[C/T]AGCAGATCAGCGCGTTACGAGCCGAGATCGCACGACTACAGATGGAGATCATGGAGTATAAAGCGGTGAGGAGGAGGAGGAGTGCACAATTAGCATCACACAATCAAAGCTGCCGTTAAATAGCATCCATAATATAAAATGTTTTGTTCATCTATCTATCAATCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCTATCCATCCATCCATCCATCCATCCATCCATCCATGAGCAATATTACACACGTAGCAATGTTGTGCCAAACCAGTGCCGATATACAGCCATATCACACTGCTACCTGTGTAATATTGCGTTTATACAACAGTTTGACAGCATAATTGTGTAATTGAAAACAAAATCAAACATGGAGAGTCTCAAAAATCCTTTTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21831
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093108 | Nonsense | 389 | 1237 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 2893419)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2845057 |
GRCz11 | 11 | 2914411 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGGTGATCGTCAACCAGGATAAAACCAGCCAGCAGATCAGCGCGTTA[C/T]GAGCCGAGATCGCACGACTACAGATGGAGATCATGGAGTATAAAGCGGTG
Long Flanking Sequence:
TCCTCCATGCAAAACTCCATGCAAAAAAACTTTTCTTCTGGAGTCAGCCGGTCTGCTTGGTCCCTCTCTAGTGCACACTGCAGTTGTTGTGCGCTGAAGGTTAATGCATGTACACAGTGTATATCAGAGGGTCACTCAGCCCACACGGGACGACACAGACAACCCATATATCCTCCTGATGTGGGTTCAGAGGGGGAGTTGATTGAATTAAACATGAGCGGCTGCAGACAGTGGCGCTGCTTTAAACGGATTCCGTCGCGTAACCATGAAACTATGCGGGCACCATGTGTGTGGTTGTGTTTATCTGTTTTGATCTCTTCTGAATGTCTTCTCGCTTTGTGTGTTTATCTAGTCGGACTGTGATGATTGCCTGCGTGAGCCCGTCTGATCGCGACTTCATGGAGACCCTGAACACGCTGAAGTATGCCAACCGGGCCCGCAACATCAAGAACAAGGTGATCGTCAACCAGGATAAAACCAGCCAGCAGATCAGCGCGTTA[C/T]GAGCCGAGATCGCACGACTACAGATGGAGATCATGGAGTATAAAGCGGTGAGGAGGAGGAGGAGTGCACAATTAGCATCACACAATCAAAGCTGCCGTTAAATAGCATCCATAATATAAAATGTTTTGTTCATCTATCTATCAATCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCTATCCATCCATCCATCCATCCATCCATCCATCCATGAGCAATATTACACACGTAGCAATGTTGTGCCAAACCAGTGCCGATATACAGCCATATCACACTGCTACCTGTGTAATATTGCGTTTATACAACAGTTTGACAGCATAATTGTGTAATTGAAAACAAAATCAAACATGGAGAGTCTCAAAAATCCTTTTGTATGAGGAACTACTTTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6188
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093108 | Nonsense | 722 | 1237 | 15 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 2902298)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2853936 |
GRCz11 | 11 | 2923290 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNNNNNNNNATGAAATAGTTCCTCTTTTTGAMTMATTTGTTTTTTAGTGT[C/A]GATGGAGAACTACACTGAAGAGAAAGCCAGTAAGGTGAAGTCYGAGTACG
Long Flanking Sequence:
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNATGTATATATATATATATATATATATATATATACATATCTATATATATAGCAAGAAATTTTTCACAGTATTTCCTATAATACTTTTTCTTCTAGAGAAAGTCACATTTATTTTATTTTGCCTATTTTTCACTGAAAGAGCTGTGATAAAAACAAACAATACTGGCTGTTCTTTGAAAAGGGGAGGGGCTACTCCCATGTTTTTGGTAAAGATTAAATATCGAATAAAAAAATACACATTTCAAAGTACTTCACGGGACCTTTAACTGTTCTGAATTTGACTGCAATGCAATAACATGCACCTTTTCTAAAGCTGCTTTGAAACAATAATTATTACTTGAAACAATAATTGAATTGAAATGTTTATTTTTGGGTGAACTGTGCAGAACTTTGTTTAACAGATGAAATAGTTCCTCTTTTTGACTCATTTGTTTTTTAGTGT[C/A]GATGGAGAACTACACTGAAGAGAAAGCCAGTAAGGTGAAGTCCGAGTACGAGAAGCGCCTGAAGGAGATGAACCGGGATCTGCTGAAGCTCCAGGCCGCACAGAAGGAGCACGCGCGTCTGCTGAAGAACCAGGGCCGATACGAGAGAGAGCTGAAGAAACTGCAGTCTGAGGTGGCCGAGATGAAGAAGGCAAAGGTGAGAGGGCATTTTTAGGAATACAGCGCCCTCTGCAGGCCATCAGGAGTGTAAACCACTACACAAATCTACTTACTACACACCATTAAAAAGCATAGCATAATAAAATGTTATTATTTGTATTGTAAAGTTTGCCAGAATTTGAAAGTATGCAGTATCGTTCATTCAAAAGATTCAAGAGTCTTTCTTTTGTCTTAAGTTGCATTAGTATATTTTTGACAGTAGCCAAAAATAAACTGTGTTGTACGGGTCAAAATTATTGATCTTTCTTTTAATGCCTAAAAACATTAGAATACTAAGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41759
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093108 | Nonsense | 941 | 1237 | 18 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 2906542)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2858180 |
GRCz11 | 11 | 2927534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTAGCAGAAAAAAGTTCCAGCGGAAGGGTCCGAGCAGCGGTTTCTCC[A/T]AGACGGCGCGTCAGAAGTGGCAGTCTCTGGAGAGGAGGATCATGGACATC
Long Flanking Sequence:
TCTTCCCTCTGTCTCTGTTGGTAAAGCGCTGTCAACAAATATTTTTCCTCCATATCCCATAATGCACAGCGCATCGGCCTACGGCAGCTGGATTAGTCTAAAAGGCGCAGTACTTTTTACGGTTGGACCCGTTTTAGTACGGATCATATTCTCACCACAAACGAACCGCTCCAGGGTTCGTTTGAAAGCGTACCGAGTCCACCTCTTCAAGCAGGTCTCGGTAGGCTTATTTGGTCCGCTTTTGGTGCGCACTCGAGTGCGATTGCTGCATTCACACCTGCCCAAACGAATCGTACCAAAAGGGGAAACGAACTCTAGTGCGATTCAATCGAACTAAATAAGGCAGGTGTGAAAGCACCCTTAATATCAGTTAGGTGCCATTCATTAGTACATGTGTGTTTGCATTCCCCTATGATCTGTAAGCGACTCAGTCTGTATCTGTGTTTGATTACAGTAGCAGAAAAAAGTTCCAGCGGAAGGGTCCGAGCAGCGGTTTCTCC[A/T]AGACGGCGCGTCAGAAGTGGCAGTCTCTGGAGAGGAGGATCATGGACATCGTCATGCAGAGAATGACCATCACTAATGTGGAGGCGGATATGGACCGCCTCATTAAGGTGACTTTAAAACAAATATCAAACACATTTAAAAATTTATCATTTACAGTTCAAGTCAAAATGATTCGCCCTCCTGTGAATATTTTTTCTTTCTCAAATATTTCCTAAATGATCTTTAACAGATTCAGGAATTTTTCACCGTATTTCCTATAATATTTTTTCTTCTGAAGAAAGTTTTAATTGTTTTATTTCAGCTAGAGTAAAAGCAGTTTTCATTTTTTATTTAACCATTTTAATGTTAATATTTTTAGTCCCCTTAAAGGGCCATGACACCCCCCACTTTCGGTTAAAGTCTACTTCAGAATGTTTTCAAAAGATGCATGATTAATGGGCGTGGAGCTCCGCGAGCATCAGGCAGGAGTGGGCGTGGCCAGCAGGGGAGAAGGGGAGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21832
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093108 | Essential Splice Site | 977 | 1237 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 2908286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2859924 |
GRCz11 | 11 | 2929278 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGAAAGCAGTTACCGTCCCATGCCTAGTCCTGATGATGTGTTGTGTCC[A/G]GAAACGCGAGGAGCTCTCAGTGCAGCAGGAGGCGCTGCTGCGTAAGAGAG
Long Flanking Sequence:
TGGAAGCTGAAATTAGCTGACAAAAGCTCAAAATTATCCAGTTTTCCCCACAATTAAAGCTGACAGGTGCTAACATTGTCTTAACTGATGCTCAACACAAACAAATCTGTTAAAATAAAAAAAAAAGTTCTCCAGGGTGTCCTGAACCTTTAAGCAATACTTGTTTTGGATTGTCTAAAGAACAAAACATCGTTATACAATGACTTGCCTAATTAGCCTAACTTAACCTAGTTAAGCCTTTAAATGTCTCTAAGCTAAATACTAGTATCTTGAAAAATATCTAGTGAAATATTATGTGCTGTCATCATGGCAAATATAAAAGAAATCAGTGATTAGAAATGAGTTAATAAAATTATTATATTTAGAAATGTGCTGAAAAAAAACAGCAATTGGGGACAAAAATATCTTTGAGCCGGTTTAAAACCTTGACTTTTCTAAACCACGGTAAACCTTGAAAGCAGTTACCGTCCCATGCCTAGTCCTGATGATGTGTTGTGTCC[A/G]GAAACGCGAGGAGCTCTCAGTGCAGCAGGAGGCGCTGCTGCGTAAGAGAGAGAAGCTGCTGAGTGAAAGCTTCAGAGAAGAGGACGAGGAGAGACTCCTGCAGGAGATGAACGAGGAGATCGAGGTGCTCAACGCTAATATAGACTACATCAGCGACAGCCTGTCTGACTGCCAGGCCACCATCGTGCAGATTGAGGAGACCAAGGTGAAGAACAATTATAGTTAATGTCAGAATTATTAGCCTTCCTGTAATTTATTTTTATTTACATTTTTTTTAAATATTTACCAAATGATGTTTAACAGATTAAATTTTTCACAGTATTTCCGATAATATTTTTTCTTCAGGAGAAAGTCTTATTTGCTTTATTTTGGCTGGAATAAAAGAAGTTTTTAATTTTTATGAAACCATTTAATAGCCCCCTTATGCAATATTTGTTTTTCGATTGTCTACAGAACAAACCATCGTTATACAATAACTTGCCTAATTACCTTAATTAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10974
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093108 | Nonsense | 1133 | 1237 | 21 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 2909712)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2861350 |
GRCz11 | 11 | 2930704 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAAGGCGGAGTGCATCCCTGAACTGCAGGCTTTAATCCATAATKTCCAA[C/T]AAGGTGAAGATTCACTTTCATTTTAGTTAATTGTGTTTCAAATAGGGCTG
Long Flanking Sequence:
TAATATTCAGCTTAGAGTGACATTTAAAGGCTTAACTAGGTTAGTTTGGCAAGTTAGGGTAATTAGACAAGTCATTGTATAACGAATCTGTAGACAATTAAAAACAAATATTGCTTAAGGGGCTAACAATATTAAGCTTAAAATGGTGTTTAAAAAATTAAAAACTGCTTTTATTCTAGCCGAAATAAAACAAATCAGACTTTCTCCAGAAGAAAAAATATTATAAAAAATACTGTGAAAAAATCCTGAATCTGTTCAACATCATTTGGGAAATATCTGAAAAAGAAAAACATTCACAGGAGGACGAATCATTGATTTTTGTTTGCTTGTCTGTATAGGGTTTACAGGTCGCCCAGAAGGAGGCTCAGATTCGCCTGCTGGAAGGTCAGCTGCGGCAGACTGATGTGATCGGCTCGTCCCATAATCACATGATCCTGGACGCTCTGAGGGAAAAGGCGGAGTGCATCCCTGAACTGCAGGCTTTAATCCATAATGTCCAA[C/T]AAGGTGAAGATTCACTTTCATTTTAGTTAATTGTGTTTCAAATAGGGCTGCAAGACATTGGAAAATATTGGAATTATAATTATTATTATTATTATTTATTCATTTATTTTCCTTCTGCTTAGTCACTTATTTATCAGGGGTCACAACAGCGGAATGAACCGCCAACTATTGCAGCATATGTTTTACACAGTGGATGTCCTTCCAGCCACAACCCAGTACTGGGAAACACCCATACACACTCATTCACACACGCTCATACACTACGGCCAATTTTGTTTAACCAATTCACCAAACCGCATGTGTTTGGACTGTGGGGGAAACCAGAGCACCCGGAGGAAACCCACGCCAACACAGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGACCCAGGCTGGATTTAATCCATGACCTTCTTGCTGTGAGGCGACAGTGCCAACCACTGAGCCACTGTGCCACCCTAATATTATCATTATTAGTATTTTTAAAAATATTAT
Associated Phenotype:
Not determined